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Merck

Cdc25 mitotic inducer targeted by chk1 DNA damage checkpoint kinase.

Science (New York, N.Y.) (1997-09-05)
B Furnari, N Rhind, P Russell
RESUMEN

Arrest of the cell cycle at the G2 checkpoint, induced by DNA damage, requires inhibitory phosphorylation of the kinase Cdc2 in both fission yeast and human cells. The kinase Wee1 and the phosphatase Cdc25, which regulate Cdc2 phosphorylation, were evaluated as targets of Chk1, a kinase essential for the checkpoint. Fission yeast cdc2-3w Deltacdc25 cells, which express activated Cdc2 and lack Cdc25, were responsive to Wee1 but insensitive to Chk1 and irradiation. Expression of large amounts of Chk1 produced the same phenotype as did loss of the cdc25 gene in cdc2-3w cells. Cdc25 associated with Chk1 in vivo and was phosphorylated when copurified in Chk1 complexes. These findings identify Cdc25, but not Wee1, as a target of the DNA damage checkpoint.

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Sigma-Aldrich
CHKtide (péptido sustrato de CHK1/CHK2), CHKtide (CHK1/CHK2 substrate peptide) primarily used in Kinase Assays.
Sigma-Aldrich
CHK1 Protein, active, 10 µg, Active, N-terminal GST tagged, human full length CHK1, for use in Kinase Assays.